Evaluating the effectiveness of deucravacitinib for plaque psoriasis in adults in France
Registry of Psoriasis Health Outcomes: A Longitudinal Real-world Collaboration (RePhlect) - A Real-world, Prospective, Observational Study of the Effectiveness of Deucravacitinib in Adults With Moderate-to-Severe Plaque Psoriasis in France
This study is testing how well deucravacitinib works for adults with moderate-to-severe plaque psoriasis in real life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 350 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Bristol-Myers Squibb Industry-sponsored |
| Drugs / interventions | deucravacitinib |
| Locations | 40 sites (Amiens and 39 other locations) |
| Trial ID | NCT06701513 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess how effective deucravacitinib is in treating adults with moderate-to-severe plaque psoriasis in real-world settings. Participants will be adults aged 18 and older who are newly starting treatment with deucravacitinib, as reported by their physicians. The study will gather data on treatment outcomes and patient experiences to better understand the drug's effectiveness outside of controlled clinical environments.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who have been diagnosed with moderate to severe plaque psoriasis and are starting treatment with deucravacitinib.
Not a fit: Patients who are currently participating in or planning to participate in another interventional clinical trial or those with prior treatment experience with deucravacitinib will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the real-world effectiveness of deucravacitinib, potentially improving treatment options for patients with plaque psoriasis.
How similar studies have performed: While this study focuses on real-world effectiveness, similar studies evaluating other psoriasis treatments have shown promising results, indicating that real-world data can be valuable in understanding treatment outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥18 years of age * Physician-reported diagnosis of moderate to severe plaque psoriasis * Be newly initiating deucravacitinib * Do not object to participate Exclusion Criteria: * Currently participating in or planning to participate in an interventional clinical trial * Previous treatment experience with deucravacitinib, including patients who received deucravacitinib as part of a blinded, randomized trial
Where this trial is running
Amiens and 39 other locations
- Local Institution - 060 — Amiens, France (Not_yet_recruiting)
- Cabinet Médical Elisabeth Lion — Angers, France (Recruiting)
- Local Institution - 045 — Argenteuil, France (Not_yet_recruiting)
- Ch Arras — Arras, France (Recruiting)
- Local Institution - 041 — Bordeaux, France (Not_yet_recruiting)
- Local Institution - 048 — Bordeaux, France (Not_yet_recruiting)
- Centre Hospitalier William Morey - Hématologie — Chalon-sur-Saône, France (Recruiting)
- CHU Dijon — Dijon, France (Recruiting)
- Local Institution - 077 — Dijon, France (Not_yet_recruiting)
- Local Institution - 011 — La Tronche, France (Not_yet_recruiting)
- Local Institution - 074 — Le Puy-en-Velay, France (Not_yet_recruiting)
- Local Institution - 039 — Lens, France (Not_yet_recruiting)
- Local Institution - 004 — Marcq-en-Barœul, France (Not_yet_recruiting)
- Local Institution - 036 — Montpellier, France (Not_yet_recruiting)
- Local Institution - 012 — Nice, France (Not_yet_recruiting)
- Local Institution - 008 — Niort, France (Not_yet_recruiting)
- Local Institution - 070 — Niort, France (Not_yet_recruiting)
- Local Institution - 062 — Nîmes, France (Not_yet_recruiting)
- Local Institution - 073 — Paris, France (Not_yet_recruiting)
- Local Institution - 078 — Périgueux, France (Not_yet_recruiting)
- Local Institution - 046 — Roubaix, France (Not_yet_recruiting)
- Local Institution - 047 — Roubaix, France (Not_yet_recruiting)
- Local Institution - 051 — Saint-Mandé, France (Not_yet_recruiting)
- Local Institution - 072 — Saint-Maur-des-Fossés, France (Not_yet_recruiting)
- Hia Sainte Anne — Toulon, France (Recruiting)
- Local Institution - 054 — Toulon, France (Not_yet_recruiting)
- Local Institution - 005 — Toulouse, France (Not_yet_recruiting)
- Local Institution - 021 — Toulouse, France (Not_yet_recruiting)
- Local Institution - 037 — Toulouse, France (Not_yet_recruiting)
- Local Institution - 061 — Vandœuvre-lès-Nancy, France (Not_yet_recruiting)
- Local Institution - 064 — Vandœuvre-lès-Nancy, France (Not_yet_recruiting)
- Local Institution - 003 — Villeurbanne, France (Not_yet_recruiting)
- Local Institution - 006 — Villeurbanne, France (Not_yet_recruiting)
- Cabinet Medical — La Chaux-de-Fonds, Switzerland (Recruiting)
- Cabinet Medical — La Chaux-de-Fonds, Switzerland (Recruiting)
- Local Institution - 007 — La Chaux-de-Fonds, Switzerland (Not_yet_recruiting)
- Local Institution - 025 — La Chaux-de-Fonds, Switzerland (Not_yet_recruiting)
- Local Institution - 029 — La Chaux-de-Fonds, Switzerland (Not_yet_recruiting)
- Local Institution - 038 — La Chaux-de-Fonds, Switzerland (Not_yet_recruiting)
- Local Institution - 044 — La Chaux-de-Fonds, Switzerland (Not_yet_recruiting)
Study contacts
- Study coordinator: BMS Study Connect Contact Center www.BMSStudyConnect.com
- Email: Clinical.Trials@bms.com
- Phone: 855-907-3286
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.